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multivi ( )  (Hubner GmbH)

 
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    Hubner GmbH multivi ( )
    Multivi ( ), supplied by Hubner GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/multivi ( )/product/Hubner GmbH
    Average 90 stars, based on 1 article reviews
    multivi ( ) - by Bioz Stars, 2026-04
    90/100 stars

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    Seed glucosinolate content in pennycress hag single, double, and triple mutants (growth chamber grown), as determined by near infrared spectroscopic (NIRS) analysis. Mutations in each allele are in parentheses after the names of the genes mutated. Error bars represent standard deviations. Different letters above columns represent statistical differences ( p <0.05) based on one-way ANOVA and Tukey’s test. n=4.

    Journal: bioRxiv

    Article Title: Creating a new oilseed crop, pennycress, by combining key domestication traits using CRISPR genome editing

    doi: 10.1101/2025.03.15.643467

    Figure Lengend Snippet: Seed glucosinolate content in pennycress hag single, double, and triple mutants (growth chamber grown), as determined by near infrared spectroscopic (NIRS) analysis. Mutations in each allele are in parentheses after the names of the genes mutated. Error bars represent standard deviations. Different letters above columns represent statistical differences ( p <0.05) based on one-way ANOVA and Tukey’s test. n=4.

    Article Snippet: Seed glucosinolate content was determined as described in Chopra et al. , using both a non-destructive Near Infrared Spectroscopic (NIRS) analyses employing a Metrohm NIRSystems NIRS XDS MultiVial Analyzer (200 mg of seed placed within 1/3 Dram Clear Glass Vials), and a more precisely quantitative wet chemistry method.

    Techniques:

    Box plot graphs of the total protein content of seeds from the various glucosinolate mutants (growth chamber grown) without ( A ) or when combined with tt8 and fae1 knockout mutations ( B ), as determined by NIR spectroscopic analysis (NIRS). n=6. Grey dots represent each sample data and red dots estimated marginal means. Means not sharing any letter are significantly different by the Sidak test at the 5% level of significance. Note that the content shown here was calculated on bulk seeds, not a single seed basis. See legend and data S1 file for mutations information.

    Journal: bioRxiv

    Article Title: Creating a new oilseed crop, pennycress, by combining key domestication traits using CRISPR genome editing

    doi: 10.1101/2025.03.15.643467

    Figure Lengend Snippet: Box plot graphs of the total protein content of seeds from the various glucosinolate mutants (growth chamber grown) without ( A ) or when combined with tt8 and fae1 knockout mutations ( B ), as determined by NIR spectroscopic analysis (NIRS). n=6. Grey dots represent each sample data and red dots estimated marginal means. Means not sharing any letter are significantly different by the Sidak test at the 5% level of significance. Note that the content shown here was calculated on bulk seeds, not a single seed basis. See legend and data S1 file for mutations information.

    Article Snippet: Seed glucosinolate content was determined as described in Chopra et al. , using both a non-destructive Near Infrared Spectroscopic (NIRS) analyses employing a Metrohm NIRSystems NIRS XDS MultiVial Analyzer (200 mg of seed placed within 1/3 Dram Clear Glass Vials), and a more precisely quantitative wet chemistry method.

    Techniques: Knock-Out